The following data is part of a premarket notification filed by Dms Laboratories with the FDA for Rapid Nft.
Device ID | K831186 |
510k Number | K831186 |
Device Name: | RAPID NFT |
Classification | Culture Media, Propagating Transport |
Applicant | DMS LABORATORIES 803 N. Front St. Suite 3 Mchenry, IL 60050 |
Product Code | JSN |
CFR Regulation Number | 866.2390 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1983-04-12 |
Decision Date | 1983-05-09 |